Metabolic Modeling Tutorial
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Metabolic Modeling Tutorial
discounted EARLY registration ends Dec 31, 2014
Metabolic Modeling Tutorial
discounted EARLY registration ends Dec 31, 2014
Metabolic Modeling Tutorial
discounted EARLY registration ends Dec 31, 2014
Metabolic Modeling Tutorial
discounted EARLY registration ends Dec 31, 2014
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MetaCyc Compound Class: a chloroaromatic compound

Superclasses: an aromatic compound
an organohalogen compound an organochlorine compound

Child Classes: a dichlorobenzoate (2)

Instances:
(R)-dichlorprop ,
(R)-mecoprop ,
(S)-dichlorprop ,
(S)-mecoprop ,
1,2,4,5-tetrachlorobenzene ,
1,2-dichlorobenzene ,
1,2-dichlorobenzene dihydrodiol ,
1,3-dichlorobenzene ,
1,4-dichlorobenzene ,
2,3-dichlorophenol ,
2,4,5-trichloro-phenoxyacetate ,
2,4,5-trichlorophenol ,
2,4,6-trichlorophenol ,
2,4-dichlorophenol ,
2,4-dichlorotoluene ,
2,5-dichloro-benzaldehyde ,
2,5-dichloro-benzyl alcohol ,
2,5-dichlorophenol ,
2,5-dichlorotoluene ,
2,6-dichlorophenol ,
2-amino-4-chlorophenol ,
2-amino-5-chlorophenol ,
2-chlorophenol ,
2-deoxy-5-keto-dihydrostreptosyl-K252c ,
2-imino-3-(7-chloro-indol-3-yl)propanoate ,
2-imino-3-(indol-3-yl)propanoate ,
3,4,5-trichlorocatechol ,
3,4,6-trichlorocatechol ,
3,4-dichloro-6-methylcatechol ,
3,4-dichlorobenzoate-cis-4,5-diol ,
3,4-dichlorotoluene ,
3,4-dichlorotoluene dihydrodiol ,
3,5,6-trichloro-2-pyridinol ,
3,5,6-trichloro-2-pyridone ,
3,5-dichloro-cis-1,2-dihydroxycyclohexa-3,5-diene ,
3,5-dichlorocatechol ,
3,6-dichloro-2-methoxybenzoate ,
3,6-dichloro-4-methyl-cis-1,2-dihydro-1,2-dihydroxycyclohexa-3,5-diene ,
3,6-dichloro-4-methylcatechol ,
3,6-dichlorocatechol ,
3-chloro-3,5-cyclohexadiene-l,2-diol-1-carboxylate ,
3-chloro-4-(3-chloro-2-nitrosophenyl)-1H-pyrrole ,
3-chloro-4-hydroxyphenylacetate ,
3-chloro-5-fluorocatechol ,
3-chloro-5-methylcatechol ,
3-chloro-6-fluorocatechol ,
3-chlorobenzaldehyde ,
3-chlorobenzene dihydrodiol ,
3-chlorobenzoate ,
3-chlorobenzoate-cis-4,5-diol ,
3-chlorobenzyl alcohol ,
3-chlorocatechol ,
3-chlorophenol ,
3-chlorotoluene ,
4,5-dichlorobenzene-1,2-diol ,
4,6-dichloro-3-methyl-cis-1,2-dihydro-1,2-dihydroxycyclohexa-3,5-diene ,
4,6-dichloro-3-methylcatechol ,
4-chlorocatechol ,
4-chlorophenol ,
4-chlorosalicylate ,
5-chloro-3,5-cyclohexadiene-l,2-diol-1-carboxylate ,
5-chloro-3-fluorocatechol ,
5-chloro-3-methylcatechol ,
5-chloro-L-tryptophan ,
5-chlorosalicylate ,
6-N-methyl-arcyriaflavin C ,
7-carboxy-K252c ,
7-chloro-L-tryptophan ,
7-hydroxy-K252c ,
N-[2-chloro-6-(4-chloro-1H-pyrrol-3-yl)phenyl]hydroxylamine ,
aminopyrrolnitrin ,
arcyriaflavin A ,
arcyriaflavin C ,
chromopyrrolate ,
dichloro-arcyriaflavin A ,
dichlorochromopyrrolate ,
diuron ,
J-104303 ,
J-109384 ,
K252a ,
linuron ,
monodechloroaminopyrrolnitrin ,
pentachlorophenol ,
pyrrolnitrin

In Reactions of unknown directionality:

Not in pathways:
RH + chloride + hydrogen peroxide + H+ = RCl + 2 H2O
an organic molecule + hypochlorous acid = an organochlorine compound + H2O


Report Errors or Provide Feedback
Please cite the following article in publications resulting from the use of MetaCyc: Caspi et al, Nucleic Acids Research 42:D459-D471 2014
Page generated by SRI International Pathway Tools version 18.5 on Sat Nov 22, 2014, biocyc14.